Centre for Gene Regulation and Expression, School of Life Sciences, University of Dundee, Dundee DD1 5EH, UK.
Dundee Imaging Facility, School of Life Sciences, University of Dundee, Dundee DD1 5EH, UK.
Mol Cell. 2020 Jul 2;79(1):155-166.e9. doi: 10.1016/j.molcel.2020.04.032. Epub 2020 May 25.
To understand gene function, the encoding DNA or mRNA transcript can be manipulated and the consequences observed. However, these approaches do not have a direct effect on the protein product of the gene, which is either permanently abrogated or depleted at a rate defined by the half-life of the protein. We therefore developed a single-component system that could induce the rapid degradation of the specific endogenous protein itself. A construct combining the RING domain of ubiquitin E3 ligase RNF4 with a protein-specific camelid nanobody mediates target destruction by the ubiquitin proteasome system, a process we describe as antibody RING-mediated destruction (ARMeD). The technique is highly specific because we observed no off-target protein destruction. Furthermore, bacterially produced nanobody-RING fusion proteins electroporated into cells induce degradation of target within minutes. With increasing availability of protein-specific nanobodies, this method will allow rapid and specific degradation of a wide range of endogenous proteins.
为了了解基因功能,可以对编码 DNA 或 mRNA 转录本进行操作,并观察其后果。然而,这些方法并不能直接影响基因的蛋白质产物,因为蛋白质产物要么被永久性地破坏,要么以蛋白质半衰期定义的速度被耗尽。因此,我们开发了一种单一成分系统,可以诱导特定内源性蛋白质本身的快速降解。一种将泛素 E3 连接酶 RNF4 的 RING 结构域与蛋白质特异性骆驼科纳米抗体相结合的构建体通过泛素蛋白酶体系统介导靶标破坏,我们将这个过程描述为抗体 RING 介导的破坏(ARMeD)。该技术具有高度特异性,因为我们没有观察到非靶向蛋白破坏。此外,电穿孔到细胞中的细菌产生的纳米抗体-RING 融合蛋白可在数分钟内诱导靶标降解。随着蛋白质特异性纳米抗体的日益普及,这种方法将允许快速和特异性降解广泛的内源性蛋白质。